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An Open-Label Study Of Lamictal In Neurotic Excoriation

An Open-Label Study of Lamictal In Neurotic Excoriation

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00269594
Enrollment
25
Registered
2005-12-23
Start date
2006-01-31
Completion date
2006-09-30
Last updated
2007-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurotic Disorders, Obsessive-Compulsive Disorder

Keywords

Skin, Picking, Pick, Neurotic Excoriation

Brief summary

The goal of the proposed study is to evaluate the efficacy and safety of Lamictal in neurotic excoriation. Twenty subjects with neurotic excoriation will receive 12 weeks of open-label treatment with Lamictal. The hypothesis to be tested is that Lamictal will be effective and well tolerated in patients with neurotic excoriation. The proposed study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.

Interventions

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* men and women age 18-65 * current diagnosis of neurotic excoriation

Exclusion criteria

* unstable medical illness or clinically significant abnormalities on prestudy laboratory tests or physical examination * history of seizures * myocardial infarction within 6 months * current pregnancy or lactation, or inadequate contraception in women of childbearing potential * a need for medication other than Lamictal with possible psychotropic effects or unfavorable interactions with Lamictal * clinically significant suicidality * lifetime history of DSM-IV bipolar disorder type I, dementia, or schizophrenia or any other DSM-IV psychotic disorder * current or recent (past 3 months) DSM-IV substance abuse or dependence * illegal substance use within 2 weeks of study initiation * initiation of psychotherapy or behavior therapy from a mental health professional within 3 months prior to study baseline * previous treatment with Lamictal * treatment with investigational medication or depot neuroleptics within 3 months, with fluoxetine within 6 weeks, or with other psychotropics within 2 weeks prior to study baseline * current treatment with an anti-epileptic medication and * patients who have previously been diagnosed with a medical condition that cause skin itchiness (e.g. liver, kidney, and blood diseases, etopic allergies)

Design outcomes

Primary

MeasureTime frame
Yale-Brown Obsessive Compulsive Scale Modified for Neurotic Excoriation

Secondary

MeasureTime frame
Skin Picking Symptom Assessment Scale (SP-SAS) and the Clinical Global Impression scale

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026